HAWTHORNE, N.Y.--(BUSINESS WIRE)--Taro Pharmaceutical Industries Ltd. (“Taro,” PINK SHEETS: TAROF) reported today that it has received final approval from the U.S. Food and Drug Administration (“FDA”) for its Abbreviated New Drug Application (“ANDA”) for Terbinafine Hydrochloride Cream 1% (“terbinafine cream”). Taro had received tentative approval for this ANDA in March 2006.
